Exenatide Affects Circulating Cardiovascular Risk Biomarkers Independently of Changes in Body Composition

被引:152
作者
Bunck, Mathijs C. [1 ]
Diamant, Michaela [1 ]
Eliasson, Bjorn [2 ]
Corner, Anja [3 ,4 ]
Shaginian, Rimma M. [5 ]
Heine, Robert J. [1 ,6 ]
Taskinen, Marja-Riitta [3 ]
Yki-Jarvinen, Hannele [3 ]
Smith, Ulf [2 ]
机构
[1] Vrije Univ Amsterdam, Med Ctr, Ctr Diabet, Dept Internal Med,Sect Endocrinol, Amsterdam, Netherlands
[2] Sahlgrens Univ Hosp, Lundberg Lab Diabet Res, Gothenburg, Sweden
[3] Univ Helsinki, Cent Hosp, Dept Med, Helsinki, Finland
[4] Minerva Med Res Inst, Helsinki, Finland
[5] Eli Lilly & Co, Houten, Netherlands
[6] Eli Lilly & Co, Indianapolis, IN 46285 USA
关键词
INSULIN GLARGINE; PEPTIDE-1; ANALOG; FAT; EXENDIN-4; LIRAGLUTIDE; METFORMIN;
D O I
10.2337/dc09-2361
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
OBJECTIVE To study the effect of exenatide on body composition and circulating cardiovascular risk biomarkers. RESEARCH DESIGN AND METHODS Metformin-treated patients with type 2 diabetes (N = 69) were randomized to exenatide or insulin glargine and treated for 1 year. Body composition was evaluated by dual-energy X-ray absorptiometry. Additionally, body weight, waist circumference, and cardiovascular biomarkers were measured. RESULTS Treatment with exenatide for 1 year significantly reduced body weight, waist circumference, and total body and trunkal fat mass by 6, 5, 11, and 13%, respectively. In addition, exenatide increased total adiponectin by 12% and reduced high-sensitivity C-reactive protein by 61%. Insulin glargine significantly reduced endothelin-1 by 7%. These changes were statistically independent of the change in total body fat mass and body weight. CONCLUSIONS Exenatide treatment for 1 year reduced body fat mass and improved the profile of circulating biomarkers of cardiovascular risk. No significant changes were seen with insulin glargine except a trend for reduced endothelin-1 levels.
引用
收藏
页码:1734 / 1737
页数:4
相关论文
共 15 条
[1]
One-year Treatment With Exenatide Improves β-Cell Function, Compared With Insulin Glargine, in Metformin-Treated Type 2 Diabetic Patients A randomized, controlled trial [J].
Bunck, Mathijs C. ;
Diamant, Michaela ;
Corner, Anja ;
Eliasson, Bjorn ;
Malloy, Jaret L. ;
Shaginian, Rimma M. ;
Deng, Wei ;
Kendall, David M. ;
Taskinen, Marja-Riitta ;
Smith, Ulf ;
Yki-Jarvinen, Hannele ;
Heine, Robert J. .
DIABETES CARE, 2009, 32 (05) :762-768
[2]
Exendin-4, a GLP-1 receptor agonist, directly induces adiponectin expression through protein kinase A pathway and prevents inflammatory adipokine expression [J].
Chung, Le Thi Kim ;
Hosaka, Toshio ;
Yoshida, Masaki ;
Harada, Nagakatsu ;
Sakaue, Hiroshi ;
Sakai, Tohru ;
Nakaya, Yutaka .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2009, 390 (03) :613-618
[3]
Beneficial effects of once-daily liraglutide, a human glucagon-like peptide-1 analogue, on cardiovascular risk biomarkers in patients with Type 2 diabetes [J].
Courreges, J. -P. ;
Vilsboll, T. ;
Zdravkovic, M. ;
Le-Thi, T. ;
Krarup, T. ;
Schmitz, O. ;
Verhoeven, R. ;
Buganova, I. ;
Madsbad, S. .
DIABETIC MEDICINE, 2008, 25 (09) :1129-1131
[5]
The association between abdominal visceral fat and carotid stiffness is mediated by circulating inflammatory markers in uncomplicated type 2 diabetes [J].
Diamant, M ;
Lamb, HJ ;
van de Ree, MA ;
Endert, EL ;
Groeneveld, Y ;
Bots, ML ;
Kostense, PJ ;
Radder, JK .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2005, 90 (03) :1495-1501
[6]
Exendin-4, a glucagon-like protein-1 (GLP-1) receptor agonist, reverses hepatic steatosis in ob/ob mice [J].
Ding, XK ;
Saxena, NK ;
Lin, SB ;
Gupta, N ;
Anania, FA .
HEPATOLOGY, 2006, 43 (01) :173-181
[7]
Horton ES, 2009, DIABETOLOGIA, V52, pS298
[8]
Weight loss with liraglutide, a once-daily human glucagon-like peptide-1 analogue for type 2 diabetes treatment as monotherapy or added to metformin, is primarily as a result of a reduction in fat tissue [J].
Jendle, J. ;
Nauck, M. A. ;
Matthews, D. R. ;
Frid, A. ;
Hermansen, K. ;
During, M. ;
Zdravkovic, M. ;
Strauss, B. J. ;
Garber, A. J. .
DIABETES OBESITY & METABOLISM, 2009, 11 (12) :1163-1172
[9]
Role of Body Fat Distribution and the Metabolic Complications of Obesity [J].
Jensen, Michael D. .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2008, 93 (11) :S57-S63
[10]
The Role of Incretins in Glucose Homeostasis and Diabetes Treatment [J].
Kim, Wook ;
Egan, Josephine M. .
PHARMACOLOGICAL REVIEWS, 2008, 60 (04) :470-512